chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108213131982131320G-1GENIChomozygous51516668
108213134682131347C-2GENIChomozygous51516669
108213769082137691C-2GENICheterozygous51516710
108213896182138962GT1GENIChomozygous52390726
108213897882138979GT1GENIChomozygous51516720
108213898382138984CT1GENIChomozygous51516721
108213899882138999GT1GENIChomozygous51516722
108213900082139001AT1GENIChomozygous51516723
108213900782139008AT3GENIChomozygous51516724
108213901982139020AT10GENIChomozygous51516725
108213917182139172A-5GENICheterozygous51516727
108213919582139196A-1GENIChomozygous51516728
108215229182152292A-2INTERGENICheterozygous52322206
108216039082160391TG1INTERGENIChomozygous51516792
108216039182160392TA1INTERGENIChomozygous51516793
108216039682160397C-1INTERGENIChomozygous51516794
108216039782160398CG1INTERGENIChomozygous52390728
108218548182185482CCA22GENICpossibly homozygous51516834